Director, Quality Operations
About the role
Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world. The Impact You Will Make The Quality Director is responsible for leading both the Quality Assurance and Quality Systems groups at the Northridge facility. The primary duty of this position is the management of the Quality Assurance and Quality Systems functions, including directing the work of subordinate managers, supervisors, and employees, and exercising independent judgment on matters of significance affecting product quality, compliance, and business operations. In this role, the Director will ensure quality systems, manufacturing support activities, and batch disposition processes operate effectively and in compliance with cGMP requirements. Additionally, this role provides leadership for site Quality Assurance operations and serves as a key partner to Manufacturing, Engineering, and Supply Chain to ensure reliable commercial production while maintaining the highest standards of compliance and patient safety. The Quality Director drives operational excellence across quality processes and develops a high-performing quality organization capable of supporting a complex multi-product contract manufacturing environment focused on transdermal and inhalation combination drug products.
Responsibilities
- Quality Leadership: Lead the daily execution of Quality Assurance and Quality System activities supporting commercial manufacturing, packaging, testing, and release activities.
- Partner closely with Manufacturing, Engineering, and Supply Chain to ensure quality support is aligned with production schedules and business priorities.
- Ensure quality systems and processes support efficient operations while maintaining compliance with applicable regulatory requirements.
- Drive a culture of quality, accountability, continuous improvement, and operational excellence throughout the organization.